Biological Sciences Department, University of Wisconsin-Parkside, Kenosha, Wisconsin, USA.
Biological Sciences Department, University of Wisconsin-Parkside, Kenosha, Wisconsin, USA
Appl Environ Microbiol. 2017 Dec 1;83(24). doi: 10.1128/AEM.01636-17. Print 2017 Dec 15.
In enteric bacteria such as , the transcription factor SgrR and the small RNA SgrS regulate the response to glucose phosphate stress, a metabolic dysfunction that results in growth inhibition and stems from the intracellular accumulation of sugar phosphates. SgrR activates the transcription of , and SgrS helps to rescue cells from stress in part by inhibiting the uptake of stressor sugar phosphates. While the regulatory targets of this stress response are well described, less is known about how the SgrR-SgrS response itself is regulated. To further characterize the regulation of the glucose phosphate stress response, we screened global regulator gene mutants for growth changes during glucose phosphate stress. We found that deleting , which encodes a regulator of the stringent response to nutrient starvation, decreases growth under glucose phosphate stress conditions. The stringent response alarmone regulator ppGpp (synthesized by RelA and SpoT) also contributes to recovery from glucose phosphate stress: as with , mutating and worsens the growth defect of an mutant during stress, although the mutant defect was only detectable under lower stress levels. In addition, mutating or and lowers expression (as measured with a P - fusion), suggesting that the observed growth defects may be due to decreased induction of the glucose phosphate stress response or related targets. This regulatory effect could occur through altered transcription, as and mutants also exhibit decreased expression of a P - fusion. Taken together, this work supports a role for stringent response regulators in aiding the recovery from glucose phosphate stress. Glucose phosphate stress leads to growth inhibition in bacteria such as when certain sugar phosphates accumulate in the cell. The transcription factor SgrR and the small RNA SgrS alleviate this stress in part by preventing further sugar phosphate transport. While the regulatory mechanisms of this response have been characterized, the regulation of the SgrR-SgrS response itself is not as well understood. Here, we describe a role for stringent response regulators DksA and ppGpp in the response to glucose phosphate stress. and mutants exhibit growth defects under glucose phosphate stress conditions. These defects may be due to a decrease in stress response induction, as deleting or and also results in decreased expression of and This research presents one of the first regulatory effects on the glucose phosphate stress response outside SgrR and SgrS and depicts a novel connection between these two metabolic stress responses.
在肠杆菌等细菌中,转录因子 SgrR 和小 RNA SgrS 调节对葡萄糖磷酸应激的反应,这是一种代谢功能障碍,导致生长抑制,源于细胞内糖磷酸盐的积累。SgrR 激活 的转录,SgrS 通过抑制应激糖磷酸盐的摄取,部分帮助细胞从应激中恢复。虽然这种应激反应的调节靶点描述得很好,但对于 SgrR-SgrS 反应本身是如何调节的了解较少。为了进一步描述葡萄糖磷酸应激反应的调节,我们筛选了全局调节基因突变体在葡萄糖磷酸应激下的生长变化。我们发现,缺失编码营养饥饿严格反应调节剂的 基因会降低葡萄糖磷酸应激条件下的生长。严格反应警报素调节剂 ppGpp(由 RelA 和 SpoT 合成)也有助于从葡萄糖磷酸应激中恢复:与 一样,突变 和 会在应激期间恶化 突变体的生长缺陷,尽管 突变体缺陷仅在较低应激水平下检测到。此外,突变 或 和 会降低 的表达(如 P -融合测量),表明观察到的生长缺陷可能是由于葡萄糖磷酸应激反应或相关靶标的诱导减少。这种调节作用可能通过改变 的转录来发生,因为 和 突变体也表现出 P -融合的表达降低。总之,这项工作支持严格反应调节剂在帮助从葡萄糖磷酸应激中恢复方面的作用。葡萄糖磷酸应激会导致 等细菌的生长抑制,当某些糖磷酸盐在细胞内积累时。转录因子 SgrR 和小 RNA SgrS 通过防止进一步的糖磷酸盐转运来缓解这种应激。虽然已经描述了这种反应的调节机制,但 SgrR-SgrS 反应本身的调节机制还不太清楚。在这里,我们描述了严格反应调节剂 DksA 和 ppGpp 在葡萄糖磷酸应激反应中的作用。 和 突变体在葡萄糖磷酸应激条件下表现出生长缺陷。这些缺陷可能是由于应激反应诱导减少所致,因为缺失 或 和 也导致 和 的表达降低。这项研究提供了葡萄糖磷酸应激反应的第一个调节作用之一,除了 SgrR 和 SgrS 之外,还描述了这两种代谢应激反应之间的新联系。